Colon Cancer: Gene >> SIX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303077
Start	45006396:45006396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650C>T
AA Mutation	p.Thr217Ile(p.T217I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303077
Start	45008773:45008773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338G>A
AA Mutation	p.Arg113His(p.R113H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303077
Start	45008833:45008833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.278T>A
AA Mutation	p.Ile93Asn(p.I93N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303077
Start	45008896:45008896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.215G>T
AA Mutation	p.Ser72Ile(p.S72I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303077
Start	45008966:45008966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145G>A
AA Mutation	p.Val49Met(p.V49M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303077
Start	45008565:45008565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149963762
CDS Mutation	c.546C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303077
Start	45006293:45006293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303077
Start	45009000:45009000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303077
Start	45006228:45006228(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.818delG
AA Mutation	p.Gly273AlafsTer25(p.G273Afs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SIX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303077
Start	45008705:45008705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406C>T
AA Mutation	p.Arg136Cys(p.R136C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303077
Start	45006185:45006185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861G>C
Mutation Classification	Silent
Feature Type	Transcript